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Series GSE267862 Query DataSets for GSE267862
Status Public on May 26, 2024
Title Pseudomonas aeruginosa Activates Quorum Sensing, Antioxidant Enzymes and Type VI Secretion in Response to Oxidative Stress to Initiate Biofilm Formation and Wound Chronicity
Organism Pseudomonas aeruginosa
Experiment type Expression profiling by high throughput sequencing
Summary Pseudomonas aeruginosa (PA) is an opportunistic pathogen frequently isolated from cutaneous chronic wounds. How PA, in the presence of oxidative stress (OS), colonizes chronic wounds and forms a biofilm is still unknown. The purpose of this study is to investigate the changes in gene expression seen when PA is challenged with the high levels of OS present in chronic wounds. We used a biofilm-forming PA strain isolated from the chronic wounds of our murine model (RPA) and performed a qPCR to obtain gene expression patterns as RPA developed a biofilm in vitro in the presence of high levels of OS, and then compared the findings in vivo, in our mouse model of chronic wounds. We found that the planktonic bacteria under OS conditions overex-pressed quorum sensing genes that are important for the bacteria to communicate with each other, antioxidant stress genes important to reduce OS in the microenvironment for survival, biofilm formation genes and virulence genes. Additionally, we performed RNAseq in vivo and identified the activation of novel genes/pathways of the Type VI Secretion System (T6SS) involved in RPA pathogenicity. In conclusion, RPA appears to survive the high OS microenvironment in chronic wounds and colonizes these wounds by turning on virulence, biofilm-forming and survival genes. These findings reveal pathways that may be promising targets for new therapies aimed at dis-rupting PA-containing biofilms immediately after debridement to facilitate the treatment of chronic human wounds.
 
Overall design RNAseq of Psuedomonas aeruginosa collected from nonchronic (control) and chronic wounds to understand the transcriptomic regulation of PA during infection in response to high levels of oxidative stress.
 
Contributor(s) Martins-Green M, Kim J
Citation(s) 38929094
Submission date May 20, 2024
Last update date Jul 31, 2024
Contact name Manuela Martins-Green
Organization name University of California, Riverside
Street address 900 University Ave
City Riverside
State/province CA
ZIP/Postal code 92521
Country USA
 
Platforms (1)
GPL33271 NextSeq 2000 (Pseudomonas aeruginosa)
Samples (18)
GSM8279974 CW24A
GSM8279975 CW24B
GSM8279976 CW24C
Relations
BioProject PRJNA1113559

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Supplementary file Size Download File type/resource
GSE267862_count_matrix.txt.gz 222.3 Kb (ftp)(http) TXT
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